UDI device identifier
VeriQuick 11012637M
UDI device identifier 00049696739344 · FOURSTAR GROUP INC.
Key facts
| Primary DI | 00049696739344 |
|---|---|
| Brand name | VeriQuick |
| Version or model | 11012637M |
| Company | FOURSTAR GROUP INC. |
| DUNS number | 656091279 |
| Product code | JXM |
| GMDN term | Benzodiazepine group IVD, kit, enzyme immunoassay (EIA) |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Jul 26, 2021 |
| Version date | Aug 3, 2021 |
| Description | MULTI-DRUG URINE TEST DIP CARD |
At a glance
- None MAUDE reports citing this UDI
- No Linked premarket submission
- No EUDAMED counterpart found
- 100–999 GUDID devices with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About UDI device identifiers (GUDID)
The Global Unique Device Identification Database (GUDID) holds the device identifiers (UDI-DIs) and key attributes that labelers submit to the FDA for devices that carry a unique device identifier.
Source: U.S. FDA Global Unique Device Identification Database (GUDID), via NLM AccessGUDID · Source date: